Are Covid-19 vaccines Arsenic Chelators?
A few days ago I published a podcast on the history of chemical warfare, drug treatments for toxic gas inhalation and arsenic removal therapies. I looked at some of the compounds natural to our bodies that can remove arsenic too.
Then it struck me, if we really are dealing with arsine gas and its various arsenic forms, why would clinicians try and reinvent the wheel? Why would they not just use arsenic chelator treatments? Are they not just making things harder for themselves?
It might LOOK good, and be financially beneficial however, to make it appear as if they HAVE completely reinvented the wheel of arsenic chelation. To some degree they may have with the introduction of lipid nanoparticles, but even those may not be quite as fantastical as we have been led to believe.
Then of course there is the necessity of continuing on the ‘virus’ (poison in latin) Merry Go Round that they have kept us on for so long. As long as that goes on there will be no overlap between Chelation and Vaccination, or will there?
VACCINES AS ARSENIC CHELATORS
So what if Covid-19 vaccines really are arsenic chelators? Here are the base ingredients of Astra Zeneca -
The adenovirus vector comes from the chimpanzee. A VIRAL VECTOR is like a cleaned out container for material that the vaccine designer wants to deliver in to the cells. It can be used to deliver DRUGS and/or PROTEINS. This viral vector attaches to cell membranes, is absorbed in to the cell wall and delivers its contents.
This Astra Zeneca vaccine also contains
L-histidine (amino acid) - this is a pH buffer and precursor to histamine, but it is also a STRONG CHELATOR OF METALS - these include toxic Fe3+ (inorganic Iron III) which is known to be released from red blood cells in arsine gas exposure, Fe2+ (iron II), Copper II (Cu2+) which can also be released by arsine gas from red blood cells and can be toxic to the liver and kidneys, Cobalt (Co2+), Nickel (Ni2+), Cadmium (Cd2+), and, Zinc (Zn2+), though we would ideally need to conserve Zinc, which is depleted by arsenic.
L-histidine hydrochloride monohydrate (amino acid) - see above.
Magnesium chloride hexahydrate (salt) - used to regulate acidity and can influence osmotic pressure in the viral vector.
Polysorbate 80 (surfactant) - This ensures even dispersal of the vaccine ingredients in solution (surfactant), and also provides protection of the active ingredients, including proteins.
Ethanol (alcohol) - trace for disinfection.
Sucrose (sugar) - maintains molecule shape.
Sodium chloride (salt).
Disodium edetate dihydrate (salt) - this is a non sulphur bonding heavy metal chelator, which can chelate toxic Fe3+ as above. It also chelates zinc. In vaccines it is apparently used to soak up any metals that leach in to the solution from the bottle and lid.
Water for injections (diluent).
So there are at least two non-arsenic Chelating agents in the Astra Zeneca Covid-19 Vaccine.
If there is no arsenic chelating agent in the vaccine, arsenic will be released on vaccination, some will be detoxified naturally but the rest will recirculate back round again, sticking to other proteins and cells. So it stands to reason that if there are non-arsenic chelating agents in the vaccine, there must be arsenic chelating agents.
SPIKE PROTEIN
In order to ‘infect a cell’ the 'spike protein' in Covid 19 ‘infection’ must apparently form a disulphide bridge with its target protein.
So, if we look at this in terms of arsenic, in effect the ‘spike protein’ could be literally ANY sulphur containing protein in the body, FOREIGN OR HUMAN, that can form disulphide bridges with arsenic.
In this paper it shows clearly that breaking the disulphide bond between the ‘spike protein’ and the ACE2 receptor, ‘blocks the virus’ from entering the cell. In other words, interrupt the strong two sulphur bond arsenic has formed between a protein and a receptor.
Because arsenic doesn't really care WHAT protein it attaches to, or which proteins it joins together, it can cause a huge amount of trouble, breaking lots of essential functions in the body including our immune response!
They tell us that this ‘spike protein’ mRNA is carried by the vaccine vector, and somehow, by miracle this monster protein (it is really really big!) is replicated by cellular machinery.
Even if the magic protein ingredients were just a small part of the supposed spike protein, in order to remove arsenic, they must contain at least two sulphurs so they can form a disulphide bridge with an arsenic atom. These structures, a simple two sulphur atom structure, make very strong bonds with arsenic.
HOW COULD A PROTEIN CHELATE ARSENIC?
In order for a protein to alert the immune system, but also make sure it is removed, it must be foreign looking enough to be flagged as NOT HUMAN.
It must also have its own independent sulphur pairs to attract arsenic to it. BUT there is still the risk of one sulphur in the protein attaching to one arsenic bound structure, and the others to other arsenic bound structures, creating even more mess!
This is exactly what makes me believe that the arsenic chelation compound, which is super tiny, smaller than an amino acid, is much more likely.
It MIGHT be that the vaccine carries a foreign protein without any sulphur to prime the immune system. That way it would not be able to stick to arsenic anywhere in the cell. But then of course it could not possibly be the ‘spike protein’ as we know that has lots of sulphur.
The arsenic chelator could then be added as a separate compound entirely, like we sometimes see separate compounds in oral drugs.
Either that or the contents of the CONTAINER aren't tricky proteins at all and just contain ARSENIC CHELATING AGENT.
So in theory the vaccine may be a NON HUMAN protein, that may or may not have double sulphurs, that may or may not be floating around in the same container with an arsenic chelating agent. Which option do you think is most likely?
DRUG ARSENIC CHELATORS
There are not many arsenic chelators on the market – BAL (toxic), DMSA and DMPA seem to be the three available under different brand names. These are usually given in cases of acute high level arsenic exposure. They come in deep muscle tissue injection and in oral form.
Given that many countries, even America, seem to suffer from high levels of arsenic exposure in their water supplies thanks to corporate activities, it seems strange that Laboratories haven't tried to reinvent the wheel on that score too, and create more lucrative drug variations.
Ah but maybe they have, in the form of vaccinations?
So it is entirely possible that one or more of these few arsenic chelating agents have been blinged up and adapted with fancy new lipid particles and a protein or two, for removal of arsenic over longer periods.
LIPID NANOPARTICLES
The lipid nanoparticles used by Pfizer and Moderna start out as complex linear lipid structures, which form a sort of holding structure for the 'spike protein' to slow its release (see video).
These particles interact with the cell surface which allows their contents to enter the cell.
Let's remember that the vaccine manufacturers like Pfizer were telling us that the lipid nanoparticles were carrying the magic messenger RNA in to the cells in the arm. From the arm it was meant to pump out Covid-19 spike protein and get the immune system to attack it.
Nice in theory.
Firstly there are so many safety nets to stop random foreign proteins being created by the cells, and the Covid Spike protein is such a monster protein, that it seems very unlikely. I talked about this in previous vaccine articles.
Secondly everyone was telling us how the 'spike protein' was literally all over the body after vaccination, not just in the arm. Why would it need to travel if the body only needed a little bit of mRNA to produce RNA to signal to the immune system.
Right, it wouldn't!
There are two other ways that lipid nanoparticles work that nobody has talked about in any depth, which, if the vaccines were actually carrying arsenic chelating compounds, would make a lot of sense.
FIRSTLY lipid nanoparticles allow delivery of DRUGS straight to the cells without the drug attaching to things it shouldn’t or being escorted out of the body by accident. This method of delivery means that many cells get a therapeutic dose throughout the body.
So if all the cells of the body are filled with arsenic, and the drug being delivered is not some fancy protein, but a simple arsenic chelating agent, it is not much use just stuck in the arm. It needs to travel!
SECONDLY lipid nanoparticles allow for the SLOW RELEASE of a drug, which is also enhanced by injecting deep in to the arm muscle. This allows the vaccine to be injected in a larger dose, than if the drug were just injected without lipid nanoparticles or container, which means it will, if injected properly, LAST LONGER!
We also heard about aspiration of needles at the injection site. As the injections are being delivered in a lipid particle, either synthetic or natural, the needle should have been aspirated in the arm before injection to ensure delivery was not in to a blood vessel. If the lipids end up in the blood stream they can cause a fat embolism, which is a blockage of the blood stream with the lipids used, and clotting will probably also occur.
Arsenic chelating drugs ALSO have a lipid base. It ensures the drug (or protein) is protected from arsenic until it is delivered in to the cell.
PANTS ON FIRE
It is important to note at this point that not only am I are pretty sure that drug companies have been telling porkie pies about the real purpose of the jabs, but so have the whistleblowers.
Various whistleblowing labs in Germany and Spain have apparently looked and found bizarre circuit board type structures and self assembling structures in their analysis of the jabs. They have also looked at blood, after extraction and exposure to oxygen, and made various comments about how badly it coagulates. Of course blood coagulates when exposed to oxygen!
My comment above, by the way, does not question the findings of those who have struggled to withdraw blood from treated people. This is an entirely separate matter, but must always be taken in conjunction with the likely presence of arsenic, irradiated arsenic and tissues and the clot forming calcium, which is known to be released in high levels in to the blood stream by arsine gas.
Just think. Are the shots that our babies are given from birth just varying doses of sulphur pair carrying proteins ready to scoop up the arsenic that they start absorbing through the placenta before birth (yes can cross the blood brain and the placental barrier)?
Is the first ‘live’ shot for measles, mumps and rubella actually just a bigger dose of chelator and/or immune triggering protein? Perhaps that vaccine is the first exposure to an actual drug based chelator?
Remember when the Pfizer boss said their computers had formulated the vaccine in just hours? Well that is perfectly feasible if all they have been doing is making tiny tweaks to the same compounds and proteins for the last 75 years! How many changes are needed in a drug to qualify it as an entirely new proprietary and money making drug?